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Chromosomal Microarray, pregnancy loss

Collection Requirements

Source: fetal tissue
Container: sterile cup or tube with sterile transport medium
Volume: 1-2 cm3


Source: maternal blood
Container: EDTA lavender

Volume:

  • Preferred: 3 mL in vacutainer
  • Minimum: 1 mL in vacutainer

Special Instructions

  • Transport at room temperature; avoid fluctuating temperatures (hot or cold)
  • Specimen must be processed within 24 hours of collection
  • Contact Genetics for collection materials
  • Use the Prenatal and Pregnancy Loss Cytogenetics Requisition

Turn Around Time

21 days

Availability

Routine

Lab Processing Instructions

Specimen: whole blood
Room temperature

Performing Laboratory

Genetics

Adele Hall Lab Section

Cytogenetics

Instrumentation/Methodology

Microarray

Additional Information

Advantages: Evaluates hundreds of different genetic conditions, including aneuploidy. Detects large and small deletions and duplications, which may not be detected by conventional chromosome analysis. Detects regions of homozygosity. DNA isolated from fresh tissue. Limitations: Cannot identify truly balanced chromosomal aberrations, i.e., balanced translocations, inversion, insertions, etc. Cannot detect point mutations or epigenetic changes. Cannot detect genomic imbalances in regions not represented on the microarray. Low-level mosaicism may not be detected.

Reference Ranges

See interpretive report

CPT

81229