Ontology highlight
ABSTRACT:
SUBMITTER: Whitby H
PROVIDER: S-EPMC2920185 | biostudies-literature | 2008
REPOSITORIES: biostudies-literature
Whitby H H Tsalenko A A Aston E E Tsang P P Mitchell S S Bayrak-Toydemir P P Hopkins C C Peters G G Bailey D K DK Bruhn L L Brothman A R AR
Cytogenetic and genome research 20080101 1-4
A database of apparently benign copy number variants (bCNVs) detected by a Spectral Genomics Inc./PerkinElmer BAC array platform has been maintained through the University of Utah Comparative Genomic Hybridization laboratory since 2005. The target population for this database represents 1,275 patients with abnormal phenotypes, primarily children referred for developmental delay and mental retardation. These bCNVs are independent of any identified copy number abnormality detected. The most common ...[more]