Variant DetailsVariant: dgv2519n100Internal ID | 20154135 | Landmark | | Location Information | | Cytoband | 15q13.2 | Allele length | Assembly | Allele length | hg38 | 195671 | hg19 | 195671 | hg18 | 195671 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1039159, nsv1048601, nsv1049759, nsv1035451, nsv1038548, nsv1040851, nsv1040948, nsv1042973, nsv1043647, nsv1041127 | Samples | | Known Genes | CHRFAM7A, LOC101059918 | 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) | dgv2519n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 23 | Observed Complex | 0 | Frequency | n/a |
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