A de novo 10q11.23q22.1 deletion detected by whole genome mate-pair sequencing: a case report.

Background: Interstitial deletions of chromosome band 10q11-q22 was a genomic disorder distinguished by developmental delay, congenital cleft palate and muscular hypotonia. The phenotypes involved were heterogeneous, hinge on the variable breakpoints and size.

Case Presentation: Here, we presented a patient with soft palate cleft, growth and development delay.