Figure 3: CNV and single-nucleotide variant DN mutations identify likely autism risk genes. | Nature Communications

Figure 3: CNV and single-nucleotide variant DN mutations identify likely autism risk genes.

From: De novo genic mutations among a Chinese autism spectrum disorder cohort

Figure 3

DN mutation patterns from SSC, AGP and ACGC samples for genes (a) TRIP12, (b) DOCK8, (c) ARHGAP32 and (d) NCOR1 identify the most likely candidate genes from larger pathogenic CNV interval. Gene numbers denote the number of RefGene entries in each corresponding CNV interval. CNV deletions (red horizontal bars) and duplications (blue bars) are shown with respect to DN LGD (red circles) and DN missense (blue circles) mutations.

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