Variant DetailsVariant: nsv580107Internal ID | 16020830 | Landmark | | Location Information | | Cytoband | 19q13.41 | Allele length | Assembly | Allele length | hg38 | 138427 | hg19 | 138427 | hg18 | 138427 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv901187 | Samples | | Known Genes | DPRX, LOC284379, MIR1283-1, MIR1323, MIR498, MIR512-1, MIR512-2, MIR515-1, MIR515-2, MIR517A, MIR518B, MIR518C, MIR518F, MIR519B, MIR519C, MIR519E, MIR520A, MIR520B, MIR520C, MIR520E, MIR520F, MIR523, MIR524, MIR525, MIR526A1, MIR526B, ZNF331 | 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) | nsv580107
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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