Variant DetailsVariant: nsv514152Internal ID | 15465846 | Landmark | | Location Information | | Cytoband | 3p14.2 | Allele length | Assembly | Allele length | hg38 | 2337 | hg19 | 2337 | hg18 | 2337 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2899055, nssv2899052, nssv2899054, nssv2899057, nssv2899062, nssv2899061, nssv2899049, nssv2899050, nssv2899063, nssv2899053, nssv2899051, nssv2899059, nssv2899064, nssv2899060, nssv2899058, nssv2899056 | Samples | NA19145, NA18870, NA18489, NA19198, NA19199, NA19128, NA18908, NA19210, NA18516, NA18907, NA19252, NA19160, NA19144, NA18501, NA18500, NA18872 | Known Genes | CADPS | 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) | nsv514152
| Frequency | Sample Size | 2366 | Observed Gain | 0 | Observed Loss | 16 | Observed Complex | 0 | Frequency | n/a |
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