Fig. 4From: Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin–Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencingMapping of microdeletions involving ARID1B. a Mapping of the microdeletions involving ARID1B. b Zoomed-in view of the microdeletions. Red bar represents microdeletionsBack to article page