Variant DetailsVariant: nssv1150336Internal ID | 15530959 | Landmark | | Location Information | | Cytoband | 19p13.3 | Allele length | Assembly | Allele length | hg38 | 488329 | hg19 | 488329 | hg18 | 488329 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv577978 | Supporting Variants | | Samples | HGDP01021 | Known Genes | BSG, C2CD4C, CDC34, FGF22, FSTL3, GZMM, HCN2, MADCAM1, MIER2, MISP, ODF3L2, PALM, POLRMT, PRSS57, RNF126, SHC2, THEG, TPGS1 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nssv1150336
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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