Variant DetailsVariant: nssv452319Internal ID | 18273034 | Landmark | | Location Information | | Cytoband | 1q23.3 | Allele length | Assembly | Allele length | hg38 | 455150 | hg19 | 455150 | hg18 | 455150 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | 1 | Merged Status | S | Merged Variants | nsv428257 | Supporting Variants | | Samples | HGDP00449 | Known Genes | ATF6, DUSP12, FCGR2A, FCGR2B, FCGR2C, FCGR3A, FCGR3B, FCRLA, FCRLB, HSPA6, HSPA7, RPL31P11 | 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) | nssv452319
| Frequency | Sample Size | 62 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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