F11 Gene Factor XI deficiency NGS Genetic Test
Short Name: Factor XI Deficiency NGS Test
Also known as: Hemophilia C, Rosenthal syndrome, Plasma thromboplastin antecedent deficiency
F11 Gene Factor XI deficiency NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 weeks. 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 identify pathogenic mutations in the F11 gene that cause Factor XI deficiency, enabling accurate diagnosis, carrier testing, and informed clinical management.
- Test Code
- 2583
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 weeks
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No specific preparation required. Provide clinical history and family pedigree during genetic counseling.
Method: Venipuncture or finger-prick
Laboratory Analysis
Blood sample collected via venipuncture or finger-prick. For FTA card, a single drop of blood is applied.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Store sample as per instructions.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify pathogenic mutations in the F11 gene that cause Factor XI deficiency, enabling accurate diagnosis, carrier testing, and informed clinical management.
How to Prepare
- Ensure proper labeling of sample
- Use sterile collection equipment
- Transport sample at ambient temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This genetic test is crucial for diagnosing Factor XI deficiency, especially in patients with unexplained bleeding or family history. Early detection guides management and genetic counseling."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted sample
- Insufficient sample volume
- Incorrect sample type or container
Understanding Your Results
Pathogenic variant detected
Confirms Factor XI deficiency; refer to hematologist for management.
No pathogenic variant detected
Factor XI deficiency unlikely; consider other causes of bleeding.
Variant of uncertain significance
Further testing or family studies recommended.
Consult a hematologist or genetic counselor if results are positive, or if bleeding symptoms persist despite negative results.
Limitations
- ⚠May not detect all types of mutations (e.g., large deletions)
- ⚠Requires genetic counseling for interpretation
- ⚠Not a substitute for functional clotting assays
Risks & Considerations
- ●Minor bruising at puncture site
- ●Rare risk of infection
- ●Psychological impact of genetic results
Interfering Factors
- ●Recent blood transfusion
- ●Contaminated sample
- ●Degraded DNA
Frequently Asked Questions
What is Factor XI deficiency?
How is the F11 Gene Factor XI Deficiency NGS Genetic Test performed?
Who should consider this test?
What is the cost of the test?
How long does it take to get results?
Is fasting required for this test?
What sample types are accepted?
Can this test detect carriers of Factor XI deficiency?
What are the limitations of the test?
Is the test available in my city?
What should I do if my test results are positive?
Is genetic counseling included with the test?
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₹20,000Reference 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.
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✓ 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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