Additional file 5: Table S2.
List of chromosomal aberrations detected by aCGH (400K) in patient B not reported in the Database of Genomic Variants (http://dgv.tcag.ca/dgv/app/home?ref=GRCh37/hg19 webcite). CNVs in non coding regions were detected on 7p12.3, 7q11.22, 19q13.11 chromosomal regions. A large region on 14q11.2 contains genes poorly characterize functionally. CNVs on 4p14 and 16q24.3 involve genes of potential interest since they have been involved in the regulation of cell growth and death.
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Frigerio et al. BMC Medical Genetics 2014 15:59 doi:10.1186/1471-2350-15-59