Table 2.

Genomic coordinates (GRCh37/hg19 assembly) of ARHGAP11B (left) and of patients reported to have a homozygous 15q13.3 microdeletion (see references indicated).

ARHGAP11B	Le Pichon et al., 2010 [58]	Endris et al., 2010 [55]	Spielmann et al., 2011 [59]	Le Pichon et al., 2013 [60]	Masurel-Paulet et al., 2014 [57]
chr15:30,918,879–30,931,023	chr15:30,931,644–32,914,281	chr15:29,085,644–32,511,004 (paternal) 1 chr15:31,122,986–32,511,004 (maternal) 1	chr15:30,971,330–32,439,084	chr15:30,931,644–32,914,281	chr15:30,938,215–32,510,863 (three patients)

¹ Patient 2.