Variant DetailsVariant: nsv606777Internal ID | 16047500 | Landmark | | Location Information | | Cytoband | 7p13 | Allele length | Assembly | Allele length | hg38 | 643 | hg19 | 643 | hg18 | 643 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv11306n54 | Supporting Variants | nssv1083404, nssv1083405, nssv1083401, nssv1083400, nssv1083403, nssv1083406, nssv1083399, nssv1083402 | Samples | | Known Genes | CAMK2B | 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) | nsv606777
| Frequency | Sample Size | 17421 | Observed Gain | 5 | Observed Loss | 3 | Observed Complex | 0 | Frequency | n/a |
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