Variant DetailsVariant: nsv976960Internal ID | 18265480 | Landmark | | Location Information | | Cytoband | 15q25.2 | Allele length | Assembly | Allele length | hg38 | 312544 | hg19 | 198491 | hg18 | 198689 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2035238, nssv2035234, nssv2035236, nssv2035232, nssv2035233, nssv2035240, nssv2035239, nssv2035237, nssv2035235, nssv2035241 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | DNM1P41, EFTUD1P1, GOLGA6L4, LOC100505679, LOC388152, LOC440300, LOC642423 | Method | Sequencing | Analysis | lineage specific fixed duplications | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv976960
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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