Variant DetailsVariant: nsv593248Internal ID | 16033971 | Landmark | | Location Information | | Cytoband | 4p16.3 | Allele length | Assembly | Allele length | hg38 | 917 | hg19 | 917 | hg18 | 917 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv8883n54 | Supporting Variants | nssv987550, nssv987551, nssv987552, nssv987534, nssv987540, nssv987527, nssv987549, nssv987546, nssv987555, nssv987531, nssv987537, nssv987558, nssv987548, nssv987545, nssv987560, nssv987530, nssv987557, nssv987535, nssv987533, nssv987559, nssv987547, nssv987541, nssv987528, nssv987542, nssv987538, nssv987556, nssv987543, nssv987553, nssv987539, nssv987529, nssv987554, nssv987536, nssv987532, nssv987544 | Samples | | Known Genes | RNF212 | 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) | nsv593248
| Frequency | Sample Size | 17421 | Observed Gain | 32 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
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