Variant DetailsVariant: nsv982335Internal ID | 18270844 | Landmark | | Location Information | | Cytoband | 9q31.2 | Allele length | Assembly | Allele length | hg38 | 10557 | hg19 | 10557 | hg18 | 10557 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2563290, nssv2563284, nssv2563285, nssv2563289, nssv2563282, nssv2563291, nssv2563286, nssv2563283, nssv2563288, nssv2563287 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | TMEM38B | Method | Sequencing | Analysis | lineage specific fixed duplications | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv982335
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|