Variant DetailsVariant: nsv606787 Internal ID | 16047510 | Landmark | | Location Information | | Cytoband | 7p13 | Allele length | Assembly | Allele length | hg38 | 487 | hg19 | 487 | hg18 | 487 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv11306n54 | Supporting Variants | nssv1083492, nssv1083479, nssv1083465, nssv1083462, nssv1083474, nssv1083454, nssv1083468, nssv1083481, nssv1083470, nssv1083484, nssv1083472, nssv1083490, nssv1083460, nssv1083456, nssv1083493, nssv1083486, nssv1083464, nssv1083457, nssv1083485, nssv1083461, nssv1083478, nssv1083487, nssv1083463, nssv1083458, nssv1083471, nssv1083475, nssv1083469, nssv1083452, nssv1083473, nssv1083459, nssv1083453, nssv1083467, nssv1083476, nssv1083455, nssv1083482, nssv1083489, nssv1083488, nssv1083477, nssv1083491, nssv1083466, nssv1083483, nssv1083480 | 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) | nsv606787
| Frequency | Sample Size | 17421 | Observed Gain | 36 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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