CHROMOFIC CHROMOSOME SNP MICROARRAY 750K HIGH RESOLUTION Test Cost 22000 Rs

CHROMOFIC CHROMOSOME SNP MICROARRAY 750K HIGH RESOLUTION Test

CHROMOFIC CHROMOSOME SNP MICROARRAY 750K HIGH RESOLUTION Test

Disease: Genetic Disorders

Method: Affymetrix CytoScanƒ?› 750K Microarray

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Sample Types
  • 4 mL (2 mL min.) whole blood in 1 lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomic Microarray Requisition Form (Form 19) is mandatory.
  • Results in : Sample Daily by 4 pm; Report 10 Working days
  • Test Cost: 22,000.00/- Rs
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CHROMOFIC CHROMOSOME SNP MICROARRAY 750K HIGH RESOLUTION Test Cost 22000 Rs

Test type Pediatrician, Physician, Gynecologist
Pre-test Information Duly filled Genomic Microarray Requisition Form (Form 19) is mandatory.
Report Delivery Sample Daily by 4 pm; Report 10 Working days
Components
Price ₹ 22000
Method Affymetrix CytoScanƒ?› 750K Microarray

CHROMOFIC CHROMOSOME SNP MICROARRAY 750K HIGH RESOLUTION Test Details

Short Description

SNP-?ÿmicroarray can identify unbalanced chromosomal abnormalities (loss and/or gain of DNA) in patients with unexplained abnormal phenotypes such as mental retardation, developmental delay, dysmorphic features, congenital anomalies, and autism. SNP-based arrays also identify long contiguous stretches of homozygosity which may suggest an increased likelihood for a recessive condition or uniparental disomy.

Test Specifications

  • Speciality: Pediatrician, Physician, Gynecologist

  • Components:

  • Department: CYTOGENETICS

  • Shipping Stability: Room Temperature: NA, Refrigerator:24 hrs, Frozen: NA

PreTest Information

Duly filled Genomic Microarray Requisition Form (Form 19) is mandatory.

Detail Description

SNP-?ÿmicroarray can identify unbalanced chromosomal abnormalities (loss and/or gain of DNA) in patients with unexplained abnormal phenotypes such as mental retardation, developmental delay, dysmorphic features, congenital anomalies, and autism. SNP-based arrays also identify long contiguous stretches of homozygosity which may suggest an increased likelihood for a recessive condition or uniparental disomy.

Frequently Asked Questions

  • What is the cost of CHROMOFIC CHROMOSOME SNP MICROARRAY 750K HIGH RESOLUTION Test?

    Cost of CHROMOFIC CHROMOSOME SNP MICROARRAY 750K HIGH RESOLUTION Test is 22000 Rs

    CHROMOFIC CHROMOSOME SNP MICROARRAY 750K HIGH RESOLUTION Test Price in India ₹ 22000

  • What is Chromosomal Microarray?

    Chromosomal microarray analysis (CMA) is a technology used for the detection of clinically significant microdeletions or duplications, with high sensitivity for submicroscopic aberrations.

  • How does CMA work?

    “Microarray” refers to a microchip-based testing platform that allows high-volume, automated analysis of many pieces of DNA at once. CMA chips use labels or probes that bind to specific chromosome regions. Computer analysis is used to compare a patient's genetic material to that of a reference sample. 

  • When should you use a CMA?

    CMA's can be used for a wide variety of purposes, from Product of Conception (POC) analysis to various neurological conditions.

    They are the first-tier test for individuals with: Developmental disabilities 

    Autism spectrum disorders

  • What does CMA not detect?

    No test can rule out all genetic diseases. Some types of variants require a different test, and some regions are technically difficult to isolate and analyze.

    CMA does not detect:

    Small changes in the sequence of single genes (point mutations)

    Tiny duplications and deletions of DNA segments within a single gene (Fragile X syndrome, for example)

  • How are results used clinically?

    CMA testing may be a gateway to getting more help for families of children with previously undiagnosed conditions. A variant found on CMA may not only provide a long-awaited explanation for a patient's clinical findings.

  • What does chromosomal microarray detect?

    Chromosomal microarray (CMA) testing looks for extra (duplicated) or missing (deleted) chromosomal segments, sometimes called copy number variants (CNVs). These include:

    Microdeletions and microduplications of chromosome segments, which are too small to see under a microscope but may contain multiple genes 

    Most abnormalities of chromosome number (trisomy, monosomy, etc.), including Down syndrome 

    Most unbalanced rearrangements of chromosome structure (translocations, etc.)

  • What is the cost of Chromosomal Microarray?

    Chromosomal Microarray costs 22000

  • How many days does it take for reports?

    Reports will take 3 weeks

₹22,000.00 ₹28,000.0021% off

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