Variant DetailsVariant: nsv573667 Internal ID | 16014390 | Landmark | | Location Information | | Cytoband | 16q24.2 | Allele length | Assembly | Allele length | hg38 | 3195 | hg19 | 3195 | hg18 | 3195 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv5309n54 | Supporting Variants | nssv863042, nssv863058, nssv863030, nssv863041, nssv863062, nssv863068, nssv863067, nssv863032, nssv863043, nssv863055, nssv863073, nssv863036, nssv863074, nssv863033, nssv863047, nssv863025, nssv863064, nssv863048, nssv863056, nssv863052, nssv863050, nssv863045, nssv863023, nssv863063, nssv863044, nssv863066, nssv863029, nssv863071, nssv863038, nssv863040, nssv863024, nssv863027, nssv863060, nssv863065, nssv863031, nssv863022, nssv863051, nssv863037, nssv863061, nssv863039, nssv863059, nssv863046, nssv863049, nssv863028, nssv863026, nssv863069, nssv863035, nssv863070, nssv863053, nssv863034, nssv863057, nssv863072, nssv863054 | Samples | | Known Genes | ZC3H18 | 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) | nsv573667
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 53 | Observed Complex | 0 | Frequency | n/a |
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