Variant DetailsVariant: nsv516966Internal ID | 15097573 | Landmark | | Location Information | | Cytoband | 9q33.3 | Allele length | Assembly | Allele length | hg38 | 16867 | hg19 | 16867 | hg18 | 16867 | hg17 | 16867 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv692573, nssv687469, nssv678208, nssv690028, nssv662788, nssv653844, nssv685062, nssv680181, nssv653525, nssv668871, nssv675043, nssv664752, nssv679818, nssv655598, nssv669396, nssv657520, nssv677761 | Samples | | Known Genes | GARNL3 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv516966
| Frequency | Sample Size | 2026 | Observed Gain | 4 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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