ClinVar Genomic variation as it relates to human health

This CNV is a 23.1 Mb deletion of 4q26q28.3, on chromosome 4, (seq[GRCh37]del(4)(q26q28.3); chr4:g.114872547_138005267del) found in a de novo state. The CNV constitutes a loss encompassing 139 genes, of which 48 are protein coding. Patients with similar gains in this region have not been reported in the peer-reviewed literature. Several individuals with smaller de novo deletions, with the largest reported CNV of 17.7 Mb, which are completely encompassed within this region in the DECIPHER database and in the primary literature who are noted to display overlapping phenotypic features, including dysmorphic features, intellectual disability, and delayed development (Wakui et al. 1991; Firth et al. 2009; Hickey et al. 2013; Fernández-Jaén et al. 2014). Additional clinical presentations reported in some patients include short stature, feeding problems, gastrointestinal and behavioral issues. A number of genes within this CNV have been associated with autosomal recessive conditions, including PRSS12, SEC24D, PLK4, IL21, EXOSC9, MFSD8, INTU, KIAA1109, BBS7, PRDM5, BBS12, FAT4, and SPATA4. In this individual, no variants that fulfil our criteria for reporting have been identified on the remaining allele. Based on the size of this CNV, the numerous genes involved, de novo state, and presence of smaller de novo CNV losses completely encompassed by this CNV in several individuals with overlapping clinical presentations, this CNV is classified as pathogenic.