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Reports Within

Parameters

Reports Within:

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Requisites
Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

The maximum days the report can be obtained for the Chromosomal Microarray 315K Test is 14 days.

What are the prerequisites for the test Chromosomal Microarray 315K Test

  • Physician order
  • Consent form signed by patient or guardian
  • Insurance authorization, if applicable
  • Payment or insurance information on file
  • No contraindications for the procedure

What are the measure values for the test Chromosomal Microarray 315K Test

  • Resolution: 315,000 markers
  • Targeted Regions: Whole genome coverage
  • Sample Type: Blood, saliva, tissue
  • Turnaround Time: 2-3 weeks
  • Technique: Oligonucleotide array comparative genomic hybridization (aCGH)

What does this test Chromosomal Microarray 315K Test identify?

Chromosomal Microarray 315K Test

The Chromosomal Microarray 315K Test is a genetic test that identifies any abnormalities or variations in a person's chromosomes. This test analyzes the entire genome for copy number variations (CNVs), which are changes in the number of copies of a particular DNA segment.

Specifically, the 315K test uses an array of DNA probes to detect deletions, duplications, and other chromosomal abnormalities that may be associated with genetic disorders, developmental delays, intellectual disabilities, and other health conditions.

By identifying these genetic changes, healthcare providers can better understand a patient's risk for certain conditions and tailor treatment and management plans accordingly. The Chromosomal Microarray 315K Test can provide valuable information for genetic counseling, prenatal testing, and personalized medicine.

Why is this test Chromosomal Microarray 315K Test taken?

Why is the Chromosomal Microarray 315K Test taken?

The Chromosomal Microarray 315K Test is taken to detect any chromosomal abnormalities or genetic mutations that may be present in an individual. This test is often used to diagnose genetic disorders, developmental delays, intellectual disabilities, and birth defects.

The test analyzes a person's DNA to identify any missing or extra chromosomal segments, as well as any small changes in the DNA sequence. This information can help healthcare providers better understand the underlying cause of a person's symptoms and provide more accurate diagnosis and treatment options.

The Chromosomal Microarray 315K Test is recommended for individuals who have unexplained developmental delays, intellectual disabilities, multiple congenital anomalies, or a family history of genetic disorders. It can also be used for prenatal testing to assess the risk of chromosomal abnormalities in a fetus.

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