Variant DetailsVariant: nssv450945Internal ID | 18274065 | Landmark | | Location Information | | Cytoband | 7p13 | Allele length | Assembly | Allele length | hg38 | 317133 | hg19 | 317133 | hg18 | 317133 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv428165 | Supporting Variants | | Samples | HGDP01087 | Known Genes | AEBP1, DBNL, GCK, LINC00957, MIR4649, MIR6837, MIR6838, MRPS24, MYL7, PGAM2, POLD2, POLM, POLR2J4, RASA4CP, SPDYE1, UBE2D4, URGCP, URGCP-MRPS24 | Method | BAC aCGH | Analysis | Copy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006). | Platform | Sanger H. sapiens Whole Genome Tile Path 28.7k v3 | Comments | | Reference | Perry_et_al_2008b | Pubmed ID | 18775914 | Accession Number(s) | nssv450945
| Frequency | Sample Size | 62 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|