Variant DetailsVariant: nsv591810Internal ID | 16032533 | Landmark | | Location Information | | Cytoband | 3q22.1 | Allele length | Assembly | Allele length | hg38 | 4193 | hg19 | 4193 | hg18 | 4193 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv8608n54 | Supporting Variants | nssv974225, nssv974220, nssv974218, nssv974217, nssv974222, nssv974221, nssv974214, nssv974224, nssv974219, nssv974216, nssv974215, nssv974223 | Samples | | Known Genes | BFSP2 | 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) | nsv591810
| Frequency | Sample Size | 17421 | Observed Gain | 7 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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