Variant DetailsVariant: nssv619660Internal ID | 15471555 | Landmark | | Location Information | | Cytoband | 14q32.31 | Allele length | Assembly | Allele length | hg38 | 3086 | hg19 | 3086 | hg18 | 3086 | hg17 | 3086 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv509550 | Supporting Variants | | Samples | NA10860 | Known Genes | SNORD114-1, SNORD114-10, SNORD114-11, SNORD114-2, SNORD114-3, SNORD114-4, SNORD114-5, SNORD114-6, SNORD114-7, SNORD114-8, SNORD114-9 | 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) | nssv619660
| Frequency | Sample Size | 4 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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