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SNP Microarray Pediatric

Important Note

Detects chromosomal imbalance that may be present in newborns or children with developmental delay/congenital anomalies/autism; genotyping in the array allows detection of uniparental disomy of autosomes, the presence of consanguinity, and the associated genomic location of recessive allele risk.

Pertinent medical findings must accompany the test request form. A Clinical Questionnaire for Reveal SNP Microarray - Pediatric must be completed.

 

 

Department

Integrated Genetics (Genzyme)

Specimen Type

Blood

Container

green-top (heparin) tube (preferred)

lavender-top (EDTA) tube (acceptable)

Standard Volume

4 mL

Minimum Volume

2 mL

Pediatric Volume

2 mL (does not allow for repeat testing)

Method

Refer to Integrated Genetics website.

Ship Temperature

Room Temperature

Stability Room Temp

Refer to Integrated Genetics website.

Stability Refrigerated

n/a

Stability Frozen

n/a

CPT Codes

81229