Fig. 1. Mapping of the 2p15p16.1 microdeletion and our case (black bar). (A) The patient’s chromosomal microarray revealed the 622 kb microdeletion of 2p16.1 (GRCh37:2:60,669,493-61,292,075), and (B) schematic representation of 2p15-p16.1 microdeletion syndrome and coding genes. Dashed box lines indicate the involved region in this study. This figure was modified from data UCSC database (GRCh37/hg19) (
https://genome.ucsc.edu).
