Genomic Unity® Whole Genome 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 genetic variants across the entire genome that may correlate with your or your child’s clinical symptoms.

The analysis includes:

• Single nucleotide variants, deletions/insertions, intronic, regulatory, and intergenic variants
• Copy number variants, duplications, deletions, regions of homozygosity, mobile element insertions, inversions, and aneuploidy
• Mitochondrial genome variants (including heteroplasmy and large deletions)
• Short tandem repeat (STR) expansions in select genes

Conditions

This test may help identify causes of rare or complex genetic disorders, neurologic conditions, metabolic diseases, or other inherited conditions.

Limitations

A positive result may indicate a predisposition or confirm presence of disease but may not predict severity or age of onset. Some genetic changes may be of uncertain significance.