Variant DetailsVariant: esv2721191Internal ID | 9955487 | Landmark | | Location Information | | Cytoband | 2q31.2 | Allele length | Assembly | Allele length | hg38 | 6940 | hg19 | 6940 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6797914, essv6844236, essv6675620, essv6672343, essv6710994, essv6810639, essv6883563, essv6707647, essv6813530, essv6707646, essv6764448, essv6675619, essv6826931, essv6962242, essv6762096, essv6859703, essv6942288, essv6953662, essv6898949, essv6683193, essv6917877, essv6942289, essv6922189, essv6807714, essv6859700, essv6825444 | Samples | SSM100, SSM027, SSM075, SSM042, SSM088, SSM002, SSM041, SSM023, SSM018, SSM062, SSM017, SSM032, SSM085, SSM072, SSM005, SSM080, SSM077, SSM076, SSM095, SSM034, SSM004, SSM063 | Known Genes | MIR548N, PRKRA | 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) | esv2721191
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 22 | Observed Complex | 0 | Frequency | n/a |
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