NIPT Microdeletion Test
Short Name: NIPT Microdeletion
Also known as: NIPT for Microdeletions, Non-Invasive Prenatal Testing for Microdeletions
NIPT Microdeletion Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Maternal Blood samples. Results in Typically 8-10 working days after sample collection.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
To screen for fetal microdeletion syndromes non-invasively, aiding in early risk assessment and guiding clinical decisions for confirmatory testing and genetic counseling.
- Test Code
- 3112
- Price
- ₹20,000
- Sample Type
- Maternal Blood
- Result Time
- Typically 8-10 working days after sample collection.
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No special preparation required. Ensure a clinician's prescription if needed.
Method: Venipuncture
Laboratory Analysis
A blood sample of 10 ml will be drawn from a vein in the arm using standard venipuncture techniques.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Resume normal activities immediately.
Timeline: Typically 8-10 working days after sample collection.
Patient Instructions
About This Test
Who Should Get This Test
To screen for fetal microdeletion syndromes non-invasively, aiding in early risk assessment and guiding clinical decisions for confirmatory testing and genetic counseling.
How to Prepare
- No fasting required
- Ambient preparation is sufficient
- Sample collected in a Streck tube for stability
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"NIPT Microdeletion screening provides valuable early insights, but always confirm with diagnostic tests for definitive diagnosis."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Improper container or labeling
Understanding Your Results
Low Risk
Low probability of the screened syndrome; routine prenatal care recommended.
High Risk
Increased probability; confirmatory testing (e.g., CVS or amniocentesis) and genetic counseling advised.
If results are high-risk, or if you have concerns about the screening, consult with a genetic counselor or obstetrician promptly for further evaluation and confirmatory testing.
Limitations
- ⚠This is a screening test, not a diagnostic test; positive results require confirmation
- ⚠Limited to selected microdeletion syndromes; does not screen for all genetic conditions
- ⚠False positives and false negatives are possible
- ⚠Not suitable for all pregnancies; consult with a clinician for eligibility
Risks & Considerations
- ●No significant risks as it is a non-invasive blood test; minimal discomfort from blood draw.
Interfering Factors
- ●High maternal BMI
- ●Multiple gestations (e.g., twins)
- ●Low fetal fraction in maternal blood
- ●Recent blood transfusion or organ transplant
Compare With Similar Tests
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Frequently Asked Questions
Is the NIPT Microdeletion test safe?
What conditions does this test screen for?
When will I receive my report?
Do I need to fast?
What happens if my result is high-risk?
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How much does the test cost?
Is this test the same as diagnostic testing?
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What is the accuracy of the NIPT Microdeletion test?
Can this test be done in multiple pregnancies?
Related Tests
Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
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