Variant DetailsVariant: nsv977706Internal ID | 18266226 | Landmark | | Location Information | | Cytoband | 15q15.3 | Allele length | Assembly | Allele length | hg38 | 1703 | hg19 | 1703 | hg18 | 1703 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2021609, nssv2021603, nssv2021610, nssv2021608, nssv2021611, nssv2021604, nssv2021607, nssv2021602, nssv2021605, nssv2021606 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | EIF3J | Method | Sequencing | Analysis | lineage specific fixed duplications | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv977706
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|