Variant DetailsVariant: nsv428361Internal ID | 18278125 | Landmark | | Location Information | | Cytoband | 19p13.3 | Allele length | Assembly | Allele length | hg38 | 179148 | hg19 | 179148 | hg18 | 179148 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv453606, nssv453610, nssv453608, nssv453611, nssv453612, nssv453607 | Samples | HGDP00462, HGDP00476, NA19181, HGDP01094, HGDP00474, HGDP00471 | Known Genes | C19orf10, DPP9, LOC100131094, LRG1, PLIN4, PLIN5, SEMA6B, TNFAIP8L1 | 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) | nsv428361
| Frequency | Sample Size | 62 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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