Variant DetailsVariant: nsv1035258Internal ID | 18777789 | Landmark | | Location Information | | Cytoband | 9q31.1 | Allele length | Assembly | Allele length | hg38 | 39286 | hg19 | 39286 | hg18 | 39286 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv7695n100 | Supporting Variants | nssv3697625, nssv3697626, nssv3697627, nssv3697630, nssv3697628, nssv3697629 | Samples | | Known Genes | MIR6130 | 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) | nsv1035258
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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