Variant DetailsVariant: dgv660n100Internal ID | 20152276 | Landmark | | Location Information | | Cytoband | 10p15.2 | Allele length | Assembly | Allele length | hg38 | 451018 | hg19 | 451018 | hg18 | 451018 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1040966, nsv1052921, nsv1043635, nsv1044287, nsv1043848, nsv1054918, nsv1035593, nsv1049655, nsv1042698, nsv1044605, nsv1041950, nsv1053719, nsv1046501, nsv1037173 | Samples | | Known Genes | PFKP | 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) | dgv660n100
| Frequency | Sample Size | 29084 | Observed Gain | 25 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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