Variant DetailsVariant: nsv6773Internal ID | 15205030 | Landmark | | Location Information | | Cytoband | 9q34.3 | Allele length | Assembly | Allele length | hg38 | 5791 | hg19 | 5791 | hg18 | 5791 | hg17 | 5791 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2824, nssv3761, nssv5195, nssv8678, nssv9476, nssv845 | Samples | NA12156, NA12878, NA18555, NA18517, NA19240, NA19129 | Known Genes | EHMT1 | Method | Sequencing | Analysis | End-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005) | Platform | Capillary | Comments | | Reference | Kidd_et_al_2008 | Pubmed ID | 18451855 | Accession Number(s) | nsv6773
| Frequency | Sample Size | 9 | Observed Gain | 6 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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