Discovery of a new class of complex genomic variation that is remarkably common

By |2022-10-31T15:34:08-04:00August 25th, 2015|Categories: Announcements, Publication|

In a recently published manuscript, we demonstrated the potential impact of complex and cryptic chromosomal abnormalities in children with early onset neuropsychiatric disorders. In this study, we find that the mainstay of genetic testing for prenatal and pediatric developmental anomalies of unknown etiology, clinical microarray to detect copy number variants (CNVs), is insufficient to detect [...]