Description
This CNV is a 4 Mb deletion of 5p15.33, on chromosome 5, (seq[GRCh37]del(5)(p15.33); chr5:g.13200_4012072del), found in a de novo state. The CNV constitutes a loss encompassing 60 genes and overlaps the well-described 5p deletion syndrome, also known as cri du chat syndrome (CdCS). CdCS has an estimated population prevalence of 1:15,000 to 1:50,000 and has been reported in more than 200 probands. Unbalanced translocations have been reported in affected individuals who inherited the derivative chromosome from a parent with a balanced translocation. Deletions ranging in size from 560 kb to 40 Mb have been observed in individuals with CdCS, and phenotypic variability has been noted in relation to the location and size of the deletion. Terminal deletions are frequently observed in affected individuals (Mainardi et al. 2001; Mainardi 2006; Nguyen et al. 2016). Common features of the syndrome include high-pitched monochromatic cry, microcephaly, broad nasal bridge, epicanthal folds, micrognathia, abnormal dermatoglyphics, and severe psychomotor and mental retardation. Additional variable features include cardiac, neurological and renal abnormalities, preauricular tags, syndactyly, hypospadias, and cryptorchidism. Based on the collective evidence, this CNV is classified as pathogenic.
| # | Sample | Method | Observation |
|---|
| Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences |
|---|
| 1 | unknown | unknown | not provided | not provided | not provided | | not provided | not provided | not provided | not provided |
