Variant DetailsVariant: nsv546977Internal ID | 15987700 | Landmark | | Location Information | | Cytoband | 1p21.1 | Allele length | Assembly | Allele length | hg38 | 51308 | hg19 | 51308 | hg18 | 51308 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv398n54 | Supporting Variants | nssv719761 | Samples | | Known Genes | AMY2A, AMY2B | 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) | nsv546977
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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