Variant DetailsVariant: nsv951203Internal ID | 16953390 | Landmark | | Location Information | | Cytoband | 9q34.3 | Allele length | Assembly | Allele length | hg38 | 208000 | hg19 | 208000 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2997039 | Samples | BILGI_BIOE | Known Genes | AGPAT2, EGFL7, FAM69B, LCN10, LCN15, LCN6, LCN8, LOC100128593, MIR126, MIR6722, SNHG7, SNORA17, SNORA43 | Method | Sequencing | Analysis | | Platform | Illumina HiSeq 2000 | Comments | | Reference | Dogan_et_al_2014 | Pubmed ID | 24416366 | Accession Number(s) | nsv951203
| Frequency | Sample Size | 1 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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