DiGeorge syndrome, and a variety of congenital malformation syndromes including Velocardiofacial (VCFS), share the deletion of chromosome 22 at 22q11. However, deletions on 10p13.14 have been shown in some patients with DGS. Know more at: http://www.creative-bioarray.com/DiGeorge-II-Satellite-Enumeration-10-Probe-FMDC-11-item-4598.htm