Variant DetailsVariant: nsv1485Internal ID | 15199362 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 247534 | hg19 | 247534 | hg18 | 247534 | hg17 | 247534 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv5548, nssv1246, nssv6625, nssv9512, nssv10930 | Samples | NA18507, NA12156, NA15510, NA19240, NA19129 | Known Genes | GOLGA8A, GOLGA8B, LPCAT4, MIR1233-1, MIR1233-2, NUTM1 | 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) | nsv1485
| Frequency | Sample Size | 9 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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