Deletion contains 37 genes i.a.: BANP (611564), ZNF469 (612078), ZFPM1 (601950), IL17C (604628), CYBA (608508), MVD (603236), SNAI3 (612741), RNF166 (617178), CTU2 (617057), PIEZO1 (611184), CDT1 (605525), APRT (102600), GALNS (612222), TRAPPC2L (610970), CBFA2T3 (603870), ACSF3 (614245), CDH15 (114019), ANKRD11 (611192) and it contains the region of the known 16q24.3 microdeletion syndrome (KBG syndrome). This evidence concerns the gene ANKRD11 and KBG syndrome.