Fig. 2From: Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin–Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencingA 6q25.3 microdeletion detected in Case 1. a 6q25.3 microdeletion was identified by array-CGH. b Seven protein-coding genes including ARID1B in the microdeletion regionBack to article page