Variant DetailsVariant: nssv747366Internal ID | 15694636 | Landmark | | Location Information | | Cytoband | 10q11.22 | Allele length | Assembly | Allele length | hg38 | 169184 | hg19 | 169334 | hg18 | 169334 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv550723 | Supporting Variants | | Samples | | Known Genes | ANXA8, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R | 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) | nssv747366
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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