Variant DetailsVariant: nsv550234Internal ID | 15990957 | Landmark | | Location Information | | Cytoband | 10p12.1 | Allele length | Assembly | Allele length | hg38 | 1257 | hg19 | 1257 | hg18 | 1257 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv744766, nssv744784, nssv744768, nssv744758, nssv744746, nssv744765, nssv744761, nssv744760, nssv744781, nssv744771, nssv744749, nssv744751, nssv744780, nssv744782, nssv744776, nssv744767, nssv744763, nssv744762, nssv744747, nssv744745, nssv744753, nssv744772, nssv744769, nssv744764, nssv744748, nssv744773, nssv744759, nssv744778, nssv744779, nssv744744, nssv744775, nssv744774, nssv744750, nssv744752, nssv744756, nssv744783, nssv744770, nssv744757, nssv744777, nssv744754, nssv744755 | Samples | | Known Genes | PDSS1 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nsv550234
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 41 | Observed Complex | 0 | Frequency | n/a |
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