Genomic Unity® Genome-Wide CNV and FMR1 Analysis

Supplementary Information

Please read the following information carefully and discuss with your healthcare provider or a genetic counselor before signing the informed consent.

Purpose

To identify chromosomal abnormalities that correlate with prenatal findings or are predicted to result in severe, early-onset genetic disorders.

This analysis includes:

• Genome-wide copy number variants (duplications/deletions), mobile element insertions, regions of homozygosity (ROH), possible uniparental disomy (UPD), inversions, unbalanced translocations, and aneuploidy. 
• Maternal cell contamination is also included in the analysis.

Conditions

This test may detect genomic abnormalities related to severe congenital conditions.

Limitations

Results may indicate a predisposition to or likelihood of early-onset disease, but not all findings can be fully interpreted. Reporting Uncertain results must be opted in by the ordering provider.