Variant DetailsVariant: esv2729807Internal ID | 9964122 | Landmark | | Location Information | | Cytoband | 10p15.3 | Allele length | Assembly | Allele length | hg38 | 411 | hg19 | 411 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6900353, essv6795649, essv6783153, essv6684768, essv6672539, essv6861918, essv6965160, essv6908483, essv6819233, essv6866661, essv6838274, essv6890947, essv6976427, essv6687991, essv6935930, essv6705873, essv6737620, essv6677450 | Samples | SSM100, SSM083, SSM071, SSM027, SSM097, SSM050, SSM088, SSM029, SSM089, SSM035, SSM032, SSM003, SSM031, SSM014, SSM068, SSM040, SSM078, SSM034 | 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) | esv2729807
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
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