Variant DetailsVariant: nsv514908Internal ID | 15466542 | Landmark | | Location Information | | Cytoband | 19p13.2 | Allele length | Assembly | Allele length | hg38 | 7674 | hg19 | 7674 | hg18 | 7674 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2843658, nssv2843654, nssv2843655, nssv2843641, nssv2843645, nssv2843643, nssv2843647, nssv2843653, nssv2843646, nssv2843657, nssv2843639, nssv2843651, nssv2843652, nssv2843642, nssv2843650, nssv2843640, nssv2843656, nssv2843648, nssv2843649, nssv2843638, nssv2843644 | Samples | NA19142, NA21634, NA19127, NA19173, NA19252, NA21718, NA18484, NA18488, NA21716, NA19153, NA19122, NA19129, NA19154, NA19141, NA19235, NA19116, NA19097, NA18852, NA21583, NA19095, NA19171 | Known Genes | ZNF846 | Method | Oligo aCGH | Analysis | ADM2 threshold = 5 | Platform | Agilent Eichler Human CNP 180K v3.0 | Comments | | Reference | Campbell_et_al_2011 | Pubmed ID | 21397061 | Accession Number(s) | nsv514908
| Frequency | Sample Size | 2366 | Observed Gain | 0 | Observed Loss | 21 | Observed Complex | 0 | Frequency | n/a |
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