Variant DetailsVariant: nssv8573Internal ID | 15188605 | Landmark | | Location Information | | Cytoband | 8q24.3 | Allele length | Assembly | Allele length | hg38 | 6394 | hg19 | 6394 | hg18 | 6394 | hg17 | 6394 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv6447 | Supporting Variants | | Samples | NA12156 | Known Genes | EXOSC4, GPAA1, MIR6847 | 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) | nssv8573
| Frequency | Sample Size | 9 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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