Variant DetailsVariant: dgv28n100Internal ID | 20151644 | Landmark | | Location Information | | Cytoband | 1p36.21 | Allele length | Assembly | Allele length | hg38 | 168677 | hg19 | 169645 | hg18 | 169645 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1012081, nsv998447, nsv1000098, nsv1003633 | Samples | | Known Genes | HNRNPCL1, LOC649330, PRAMEF1, PRAMEF10, PRAMEF11, PRAMEF2, PRAMEF4, PRAMEF6, PRAMEF7, PRAMEF8 | Method | SNP array | Analysis | Affymetrix SNP array copy number analysis | Platform | Affymetrix SNP Array 6.0 | Comments | | Reference | Coe_et_al_2014 | Pubmed ID | 25217958 | Accession Number(s) | dgv28n100
| Frequency | Sample Size | 29084 | Observed Gain | 12 | Observed Loss | 73 | Observed Complex | 0 | Frequency | n/a |
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