Variant DetailsVariant: nsv1036896Internal ID | 18779427 | Landmark | | Location Information | | Cytoband | 14q11.2 | Allele length | Assembly | Allele length | hg38 | 57578 | hg19 | 57578 | hg18 | 57578 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1802n100 | Supporting Variants | nssv3531983, nssv3531971, nssv3531980, nssv3531979, nssv3531976, nssv3531978, nssv3531982, nssv3531974, nssv3531975, nssv3531977, nssv3531981, nssv3531973, nssv3531972 | Samples | | Known Genes | ECRP | 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) | nsv1036896
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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