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ARRAYCHROME PANEL

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NABL Cap Accredited 
The ArrayChrome Panel at Metropolis Healthcare is a high-resolution chromosomal microarray test designed to detect microdeletions, microduplications, and copy number variations (CNVs) associated with developmental delays, congenital anomalies, and genetic syndromes. Metropolis uses advanced microarray technology and expert genetic interpretation to ensure precise and clinically meaningful results.

  • 17 Crores+ Samples Processed
  • World Class Technology Labs
  • 25+ Years of Trust & Experience
  • Free Home Collection

Price: Rs. 17,500.00

Sample Type: EDTA Blood

Fasting Not Requierd


Frequently Asked Questions (FAQ's):

What is the ArrayChrome Panel?
It is a chromosomal microarray test at Metropolis Healthcare that identifies small chromosomal changes not detectable through traditional karyotyping.

Who should consider this test?
Individuals with developmental delay, intellectual disability, congenital malformations, autism spectrum disorder, or suspected genetic syndromes may benefit from this test.

What type of sample is required?
A blood sample is typically used, though the panel may also be performed on fetal or tissue samples if clinically indicated.

What conditions can the ArrayChrome Panel detect?
It detects microdeletions, microduplications, copy number variations, and other chromosomal imbalances linked to genetic disorders.

How is this test different from a routine karyotype?
ArrayChrome provides much higher resolution, identifying abnormalities that karyotyping cannot detect.

How accurate are results from Metropolis Healthcare?
Metropolis ensures high accuracy using advanced microarray platforms, strict laboratory quality processes, and interpretation by experienced clinical geneticists.

Is fasting required before the test?
No fasting or special preparation is needed for this genetic analysis.

How does this test help in clinical management?
Results guide diagnosis, genetic counseling, treatment planning, and long-term care decisions for children and adults with suspected genetic abnormalities.

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