Fig. 3
From: Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank
Karyograms showing location and density of deletion and duplication CNVs identified in the AAB cohort. Red density track represents CNVs detected in the ASD subset. Blue density track represents CNVs detected in the non-ASD subset (undiagnosed siblings, unrelated undiagnosed children, and parents), noting that there are instances in which parents have CNVs overlapping ASD/ID-associated regions. Yellow regions depict ASD/ID-associated CNVs from ClinGen [47] and DECIPHER [48, 49] (Additional file 2: Table 7a). Green regions denote ASD/ID/DD-associated genes reported by Satterstrom et al. [12] and DDD [50] (Additional file 2: Table 7b). Karyogram generated using the karyoploteR package [55]