Variant DetailsVariant: esv2729540Internal ID | 9963855 | Landmark | | Location Information | | Cytoband | 10p15.3 | Allele length | Assembly | Allele length | hg38 | 835 | hg19 | 835 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6958613, essv6866660, essv6779089, essv6887709, essv6862675, essv6809093, essv6895765, essv6923923, essv6935907, essv6749397, essv6740740, essv6720328 | Samples | SSM075, SSM011, SSM018, SSM096, SSM026, SSM089, SSM003, SSM067, SSM044, SSM052, SSM056, SSM012 | Known Genes | ADARB2 | 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) | esv2729540
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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