Variant DetailsVariant: nsv589416Internal ID | 16030139 | Landmark | | Location Information | | Cytoband | 3p26.1 | Allele length | Assembly | Allele length | hg38 | 12781 | hg19 | 12781 | hg18 | 12781 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv8177n54 | Supporting Variants | nssv958015, nssv958013, nssv1152448, nssv958010, nssv958012, nssv1152449, nssv1152451, nssv958014, nssv958011, nssv1152450 | Samples | NINDS_115, HGDP01357, NINDS_223, NINDS_51 | Known Genes | | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nsv589416
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
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