Variant DetailsVariant: esv2723646Internal ID | 9957946 | Landmark | | Location Information | | Cytoband | 21q22.3 | Allele length | Assembly | Allele length | hg38 | 357 | hg19 | 357 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6679073, essv6675121, essv6921642, essv6868661, essv6682770, essv6801556 | Samples | SSM089, SSM017, SSM032, SSM031, SSM033, SSM072 | Known Genes | TRPM2 | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | esv2723646
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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