NIPT Test: Fast & Precise Non-Invasive Prenatal Test
First of all, the NIPT Test (Non-Invasive Prenatal Testing) is an advanced cell-free fetal DNA screening test performed as early as week 10 of pregnancy. Essentially, Next-Generation Sequencing (NGS) of maternal blood isolates placental DNA to evaluate fetal chromosomes with over 99% accuracy. As a result, expectant parents screen for Down syndrome, Edwards syndrome, and Patau syndrome without any risk of miscarriage.
Book your NIPT Test at Henotic Diagnostics for reliable prenatal peace of mind. Furthermore, our accredited diagnostic facility operates 24/7 with dedicated home sample collection services.
📋 Your NIPT Test at a Glance
| 🔍 Detail | 📋 Info |
|---|---|
| 🩺 Technology | Cell-Free Fetal DNA (cfDNA) Next-Generation Sequencing |
| 🩸 Sample Type | 10 ml Maternal Blood in cfDNA Preservation Tube |
| 💰 Price Range | ₹14,500 – ₹24,500 (All-inclusive diagnostic fee) |
| 📄 Report TAT | 5 to 7 Days (Includes geneticist interpretation) |
| 🕐 Gestational Age | From 10 Weeks Onward (Singles & Twins) |
| 👩⚕️ Specialist | Dr. Pratibha Patil — Chief Consultant Radiologist |
| 🍽️ Fasting | No Fasting Required (Normal diet allowed) |
| 💳 Insurance | Reimbursement Documentation Support provided |
| 🏅 Accreditation | NABL Accredited · ISO Certified · PCPNDT Compliant |
NIPT Test Quality Standards & Certifications
Overview of NIPT Non-Invasive Prenatal Testing
To begin with, the NIPT Test represents the safest and most accurate non-invasive screening method for fetal chromosomal conditions. At the same time, experts at Henotic Diagnostics analyze cell-free fetal DNA (cfDNA) circulating in maternal plasma to deliver clinical clarity.
What Does NIPT Test Evaluate?
Specifically, NIPT evaluates fetal chromosomal counts for Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), Trisomy 13 (Patau syndrome), sex chromosome aneuploidies (Turner 45,X, Klinefelter 47,XXY), and microdeletions. Consequently, obstetricians provide high-precision screening without risking invasive procedures. Furthermore, high-depth NGS achieves >99.9% negative predictive value. As a result, expectant mothers enjoy complete peace of mind. In fact, to review clinical guidelines, consult the ACOG Prenatal Screening resource.
Furthermore, comfortable reception lounge ensuring a calm, stress-free sample collection for pregnant mothers
What is an NIPT Test?
In general, NIPT is a revolutionary screening technology that analyzes fragments of placental DNA present in maternal blood. Essentially, placental cell-free fetal DNA enters maternal circulation by week 7 and reaches sufficient concentration (>4% fetal fraction) by week 10. Specifically, Next-Generation Sequencers count relative chromosome ratios in blood plasma. Therefore, bioinformatic algorithms determine whether fetal trisomy risk is low or elevated. Additionally, NIPT avoids invasive needle insertion into the amniotic sac.
Additionally, high-throughput NGS platform measures cell-free fetal DNA ratios with extreme sensitivity
What Does an NIPT Test Check?
Overall, NIPT screening evaluates core autosomal trisomies, sex chromosome conditions, and structural microdeletions:
Key Chromosomal Conditions Screened
In addition, advanced bioinformatic software calculates precise risk scores for Trisomies 21, 18, and 13
When Is NIPT Test Recommended?
For example, obstetricians and maternal-fetal specialists recommend NIPT screening for all expectant mothers starting at 10 weeks gestation. In particular, NIPT is strongly advised for mothers aged 35 or older at delivery. Moreover, it is recommended if double marker serum screening or NT ultrasound indicates intermediate or high risk. In addition, mothers with a prior pregnancy affected by trisomy select NIPT for early reassurance.
Moreover, expert genetic counseling helps expectant couples understand NIPT risk reports with complete confidence
Clinical Distinction: NIPT Screening vs. Invasive Amniocentesis
Ideally, mothers should start with non-invasive NIPT if they wish to avoid the 1 in 200 procedure-related miscarriage risk of amniocentesis. In addition, if NIPT returns low risk, invasive procedures are completely avoided. Indeed, non-invasive testing offers maximum safety for your baby.
NIPT Test Cost Guide
| Prenatal Diagnostic Service | Approximate Cost (₹) |
|---|---|
| NIPT Test Basic (Trisomies 21, 18, 13) | First, basic NIPT test pricing is ₹14,500 – ₹18,500. |
| NIPT Test Advanced (Trisomies + Microdeletions) | Second, advanced NIPT panel costs ₹20,500 – ₹24,500. |
| Twin Gestation NIPT Test | In addition, twin pregnancy NIPT costs ₹18,500 – ₹22,500. |
| Pre & Post-Test Genetic Counseling | Finally, expert genetic consultation fee is ₹1,000 – ₹1,500. |
Comparison: NIPT Test vs. First Trimester Combined Screening
On one hand, First Trimester Combined Double Marker screening achieves only 85-90% detection with a 5% false positive rate, whereas NIPT achieves >99% detection with less than 0.1% false positives. Consequently, NIPT significantly reduces unnecessary invasive procedures.
| Feature | NIPT Test (cfDNA NGS) | Combined Serum Marker Screening |
|---|---|---|
| Down Syndrome Sensitivity | First, NIPT achieves >99% detection sensitivity. | However, Double Marker detects only 85% – 90%. |
| False Positive Rate | Second, NIPT false positive rate is extremely low (<0.1%). | In contrast, serum screening has a 5% false positive rate. |
| Earliest Testing Window | In addition, NIPT is performed from 10 weeks gestation. | Meanwhile, serum screening is performed at 11-13 weeks. |
| Fetal Miscarriage Risk | Finally, zero procedure-related risk to pregnancy. | Likewise, zero procedure-related risk (blood draw). |
Frequently Asked Questions
Is an NIPT Test safe for my baby? ▼
However, routine maternal blood draw carries zero risk of miscarriage for the fetus.
Do I need to fast before an NIPT Test? ▼
Because cell-free fetal DNA sequencing is independent of blood glucose, fasting is unnecessary.
How early in pregnancy can I get an NIPT Test? ▼
Generally, NIPT testing is performed accurately from 10 weeks of pregnancy onward.
How long until I receive diagnostic results? ▼
Fortunately, detailed clinical NIPT reports are delivered within 5 to 7 business days.
What is the cost of an NIPT Test? ▼
Overall, a high-precision NIPT Test ranges from ₹14,500 to ₹24,500 all-inclusive.
Quick Appointment Booking
Schedule your NIPT Test with accredited prenatal genomic experts.
Call: 088793 27184 WhatsApp BookingTest Summary
Reporting Fetal Medicine Specialist
Dr. Pratibha Patil
Chief Consultant Radiologist & Clinical Diagnostics Specialist
MBBS, MD (Radiodiagnosis) · 15+ Years Clinical Experience
Furthermore, your NIPT Test cell-free fetal DNA data is evaluated by senior fetal medicine specialists and geneticists following PCPNDT guidelines. Consequently, detailed reports provide obstetricians with trustworthy clinical guidance.
Our Accreditations & Quality Standards
Certified excellence ensuring prenatal screening sensitivity, fetal fraction accuracy, and patient privacy.
What Our Patients Say
Real feedback from expectant parents who completed NIPT testing with us.
“At 36 years old, getting an NIPT Test gave us complete anxiety relief. Furthermore, Dr. Pratibha Patil’s team provided our report within 5 days with zero hassle.”
– Meera G.
Verified Patient Review“The home phlebotomy sample collection was extremely smooth and comfortable. In addition, the genetic counselor answered every question.”
– Kavita R.
Verified Patient Review“Transparent price and PCPNDT compliant facility. Our gynecologist specifically recommended Henotic Diagnostics for NIPT.”
– Sameer D.
Verified Patient ReviewRelevant Diagnostic Prenatal & Genetic Services
Corporate Booking Office & Location
If you require an NIPT Test for non-invasive prenatal screening, do not delay. Call to schedule your sample collection.
Henotic Diagnostics
Second floor, Millennium Empire, Business Park, Plot No 47, D Mart Rd, Sector 15, Kharghar, Navi Mumbai, Panvel, Maharashtra 410210
Phone: 088793 27184 | Hours: Open 24 Hours