Variant DetailsVariant: nsv515121Internal ID | 15466755 | Landmark | | Location Information | | Cytoband | 9q32 | Allele length | Assembly | Allele length | hg38 | 202601 | hg19 | 202601 | hg18 | 202601 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2969266, nssv2969263, nssv2969264, nssv2969268, nssv2969261, nssv2969260, nssv2969267, nssv2969262, nssv2969265, nssv2969259 | Samples | NA19204, NA21365, NA21523, NA19209, NA18867, NA19210, NA21439, NA21438, NA21366, NA19211 | Known Genes | INIP, KIAA1958, SNX30 | 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) | nsv515121
| Frequency | Sample Size | 2366 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|