Variant DetailsVariant: nsv7637Internal ID | 15205980 | Landmark | | Location Information | | Cytoband | 11p15.5 | Allele length | Assembly | Allele length | hg38 | 8826 | hg19 | 8826 | hg18 | 8826 | hg17 | 8826 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv10789, nssv978, nssv6431, nssv5335, nssv1917, nssv11246, nssv9937, nssv3913 | Samples | NA18507, NA12156, NA12878, NA18956, NA15510, NA18555, NA19240, NA19129 | Known Genes | AP2A2, MUC6 | Method | Sequencing | Analysis | End-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005) | Platform | Capillary | Comments | | Reference | Kidd_et_al_2008 | Pubmed ID | 18451855 | Accession Number(s) | nsv7637
| Frequency | Sample Size | 9 | Observed Gain | 8 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|