Fig. 4
From: Genetic underpinnings explored: OPA1 deletion and complex phenotypes on chromosome 3q29
Exome sequencing and Chromosomal microarray analysis. (A) Approximately 50% fewer reads were observed in the OPA1 gene in the proband’s sample compared to two other unrelated reference samples. (B) The reads in the neighboring genes showed similar patterns between the proband and the two unrelated reference samples. (C) Chromosomal microarray analysis showed a deletion of 960 kb on chromosome 3q29