Variant DetailsVariant: nsv962871Internal ID | 18251427 | Landmark | | Location Information | | Cytoband | 22q11.23 | Allele length | Assembly | Allele length | hg38 | 294383 | hg19 | 294383 | hg18 | 294383 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2760057, nssv2758115, nssv2762271, nssv2764046, nssv2761503, nssv2762882, nssv2759269, nssv2760304, nssv2757299 | Samples | HGDP01284, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | CRYBB2P1, IGLL3P, LRP5L, MIR6817 | Method | Sequencing | Analysis | Human CNVs | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv962871
| Frequency | Sample Size | 10 | Observed Gain | 9 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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