Variant DetailsVariant: nssv2998800Internal ID | 16945066 | Landmark | | Location Information | | Cytoband | 17q25.1 | Allele length | Assembly | Allele length | hg38 | 209144 | hg19 | 209100 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv952367 | Supporting Variants | | Samples | BILGI_BIOE | Known Genes | FADS6, FDXR, GRIN2C, HID1, NAT9, OTOP2, OTOP3, SLC9A3R1, TMEM104, USH1G | Method | Sequencing | Analysis | | Platform | Illumina HiSeq 2000 | Comments | | Reference | Dogan_et_al_2014 | Pubmed ID | 24416366 | Accession Number(s) | nssv2998800
| Frequency | Sample Size | 1 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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