Variant DetailsVariant: nsv981526Internal ID | 18270037 | Landmark | | Location Information | | Cytoband | 7q11.23 | Allele length | Assembly | Allele length | hg38 | 88754 | hg19 | 88731 | hg18 | 88731 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2464970, nssv2464971, nssv2464966, nssv2464973, nssv2464968, nssv2464967, nssv2464972, nssv2464975, nssv2464974, nssv2464969 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | GTF2IP1, LOC100093631, NCF1B | Method | Sequencing | Analysis | lineage specific fixed duplications | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv981526
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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