Supplementary Figure 1 : De novo 4-bp ADNP frameshift deletion (chr20:49508752_49508755delTTTA) detected in patient 1.

From: A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP

Supplementary Figure 1

(a) WES data: IGV overview of reads for the patient and both parents. The 4-bp deletion is indicated by thin black lines. (b) Sanger sequencing confirmation of the de novo 4-bp deletion (black rectangle) in the patient and both parents.