Variant DetailsVariant: nsv6402Internal ID | 15204622 | Landmark | | Location Information | | Cytoband | 8q24.22 | Allele length | Assembly | Allele length | hg38 | 10276 | hg19 | 10276 | hg18 | 10276 | hg17 | 10276 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv10643 | Samples | NA18956 | Known Genes | MIR7848, SLA, TG | 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) | nsv6402
| Frequency | Sample Size | 9 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|