Variant DetailsVariant: nsv509639Internal ID | 15477137 | Landmark | | Location Information | | Cytoband | 16q24.3 | Allele length | Assembly | Allele length | hg38 | 14782 | hg19 | 14782 | hg18 | 14782 | hg17 | 14782 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv619698 | Samples | NA10860 | Known Genes | CDK10, CHMP1A, CPNE7, DPEP1, FANCA, RPL13, SNORD68, SPATA2L, SPATA33, SPG7, VPS9D1, VPS9D1-AS1, ZNF276 | Method | Optical mapping | Analysis | Single-molecule optical maps were assembled into genome-wide consensus maps. These consensus maps were compared to a restriction map generated from the NCBI b35 human genome reference sequence. | Platform | Optical Mapping | Comments | | Reference | Teague_et_al_2010 | Pubmed ID | 20534489 | Accession Number(s) | nsv509639
| Frequency | Sample Size | 4 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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