MYO16 and Global developmental delay: In addition, the DECIPHER database [10–11] lists a 3.83 Mb copy number loss (chr13: 106,884,343–110,711,191; NCBI Build 36) including the MYO16 gene in a male patient with global developmental delay and an apparently pathogenic maternally inherited 6.68 Mb CNV (chr13: 102,864,674–109,548,530; NCBI Build 36) in a female patient with ID, seizures and moderate behavioral/psychiatric abnormality (Table 3).