esv3989587
- Organism: Homo sapiens
- Study:estd229 (Fakhro et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array, Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:57
- Validation:Not tested
- Clinical Assertions: No
- Region Size:57,642
- Publication(s):Fakhro et al. 2015
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 896 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 907 SVs from 89 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3989587 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 97,180,422 | 97,238,063 |
| esv3989587 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 97,846,159 | 97,903,800 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| essv25966494 | deletion | DGMQ-31556 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,506 |
| essv25899193 | deletion | DGMQ-31625 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,558 |
| essv25902781 | deletion | DGMQ-32215 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,575 |
| essv25920794 | deletion | DGMQ-32061 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,712 |
| essv25937919 | deletion | DGMQ-31029 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,562 |
| essv25954439 | deletion | DGMQ-31609 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,567 |
| essv25970633 | deletion | DGMQ-31513 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,620 |
| essv25973329 | deletion | DGMQ-31416 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,428 |
| essv25982135 | deletion | DGMQ-31614 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,654 |
| essv25990866 | deletion | DGMQ-31449 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,630 |
| essv26001354 | deletion | DGMQ-32250 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,486 |
| essv26004977 | deletion | DGMQ-32064 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,555 |
| essv26017239 | deletion | DGMQ-31714 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,443 |
| essv26018863 | deletion | DGMQ-31470 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,613 |
| essv26030871 | deletion | DGMQ-32308 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,712 |
| essv26030473 | deletion | DGMQ-31274 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,454 |
| essv25897596 | deletion | DGMQ-31644 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,419 |
| essv25900929 | deletion | DGMQ-31607 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,655 |
| essv25939664 | deletion | DGMQ-32293 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,587 |
| essv25939872 | deletion | DGMQ-31131 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,468 |
| essv25944865 | deletion | DGMQ-31030 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,644 |
| essv25999612 | deletion | DGMQ-31125 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,569 |
| essv26034385 | deletion | DGMQ-31606 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,677 |
| essv25989022 | deletion | DGMQ-32182 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,451 |
| essv25895752 | deletion | DGMQ-31230 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,666 |
| essv25957832 | deletion | DGMQ-31433 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,606 |
| essv25971630 | deletion | DGMQ-32118 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,534 |
| essv25986166 | deletion | DGMQ-32182 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 0 | 1,451 |
| essv26030600 | deletion | DGMQ-32308 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 0 | 1,712 |
| essv25966495 | deletion | DGMQ-31556 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,506 |
| essv25937920 | deletion | DGMQ-31029 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,562 |
| essv25964333 | deletion | DGMQ-31129 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,496 |
| essv25973330 | deletion | DGMQ-31416 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,428 |
| essv25937921 | deletion | DGMQ-31029 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,562 |
| essv25954689 | deletion | DGMQ-31177 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,445 |
| essv25956143 | deletion | DGMQ-32287 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,502 |
| essv25959607 | deletion | DGMQ-31711 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,479 |
| essv25969750 | deletion | DGMQ-31123 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,704 |
| essv25974921 | deletion | DGMQ-31623 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,664 |
| essv25997832 | deletion | DGMQ-31568 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,594 |
| essv26020682 | deletion | DGMQ-32302 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,531 |
| essv26030872 | deletion | DGMQ-32308 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,712 |
| essv25939665 | deletion | DGMQ-32293 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,587 |
| essv25985752 | deletion | DGMQ-31508 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,545 |
| essv26022349 | deletion | DGMQ-31724 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,583 |
| essv25906158 | deletion | DGMQ-31005 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,544 |
| essv25904487 | deletion | DGMQ-31237 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,475 |
| essv25939883 | deletion | DGMQ-31131 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,468 |
| essv25948630 | deletion | DGMQ-31105 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,808 |
| essv25952617 | deletion | DGMQ-31639 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,641 |
| essv25964663 | deletion | DGMQ-31617 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,636 |
| essv25982136 | deletion | DGMQ-31614 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,654 |
| essv25990868 | deletion | DGMQ-31449 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,630 |
| essv25999613 | deletion | DGMQ-31125 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,569 |
| essv26001356 | deletion | DGMQ-32250 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,486 |
| essv26038064 | deletion | DGMQ-31725 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,478 |
| essv26004988 | deletion | DGMQ-32064 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,555 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv25966494 | Remapped | Perfect | NC_000002.12:g.(97 180422_?)_(?_97184 142)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,180,422 | 97,184,142 |
| essv25899193 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv25902781 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv25920794 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv25937919 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv25954439 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv25970633 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv25973329 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv25982135 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv25990866 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv26001354 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv26004977 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv26017239 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv26018863 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv26030871 | Remapped | Perfect | NC_000002.12:g.(97 181627_?)_(?_97185 349)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,627 | 97,185,349 |
| essv26030473 | Remapped | Perfect | NC_000002.12:g.(97 181814_?)_(?_97238 063)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,181,814 | 97,238,063 |
| essv25897596 | Remapped | Perfect | NC_000002.12:g.(97 182664_?)_(?_97185 547)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,182,664 | 97,185,547 |
| essv25900929 | Remapped | Perfect | NC_000002.12:g.(97 182664_?)_(?_97185 547)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,182,664 | 97,185,547 |
| essv25939664 | Remapped | Perfect | NC_000002.12:g.(97 182664_?)_(?_97185 547)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,182,664 | 97,185,547 |
| essv25939872 | Remapped | Perfect | NC_000002.12:g.(97 182664_?)_(?_97185 547)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,182,664 | 97,185,547 |
| essv25944865 | Remapped | Perfect | NC_000002.12:g.(97 182664_?)_(?_97185 547)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,182,664 | 97,185,547 |
| essv25999612 | Remapped | Perfect | NC_000002.12:g.(97 182664_?)_(?_97185 547)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,182,664 | 97,185,547 |
| essv26034385 | Remapped | Perfect | NC_000002.12:g.(97 182664_?)_(?_97185 547)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,182,664 | 97,185,547 |
| essv25989022 | Remapped | Perfect | NC_000002.12:g.(97 184225_?)_(?_97187 976)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,184,225 | 97,187,976 |
| essv25895752 | Remapped | Perfect | NC_000002.12:g.(97 187664_?)_(?_97190 363)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,187,664 | 97,190,363 |
| essv25957832 | Remapped | Perfect | NC_000002.12:g.(97 187664_?)_(?_97190 363)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,187,664 | 97,190,363 |
| essv25971630 | Remapped | Perfect | NC_000002.12:g.(97 187664_?)_(?_97190 363)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,187,664 | 97,190,363 |
| essv25986166 | Remapped | Perfect | NC_000002.12:g.(97 188114_?)_(?_97190 363)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,188,114 | 97,190,363 |
| essv26030600 | Remapped | Perfect | NC_000002.12:g.(97 188114_?)_(?_97190 363)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,188,114 | 97,190,363 |
| essv25966495 | Remapped | Perfect | NC_000002.12:g.(97 188114_?)_(?_97190 813)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,188,114 | 97,190,813 |
| essv25937920 | Remapped | Perfect | NC_000002.12:g.(97 188564_?)_(?_97190 813)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,188,564 | 97,190,813 |
| essv25964333 | Remapped | Perfect | NC_000002.12:g.(97 188564_?)_(?_97190 813)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,188,564 | 97,190,813 |
| essv25973330 | Remapped | Perfect | NC_000002.12:g.(97 192916_?)_(?_97215 530)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,192,916 | 97,215,530 |
| essv25937921 | Remapped | Perfect | NC_000002.12:g.(97 199309_?)_(?_97203 047)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,199,309 | 97,203,047 |
| essv25954689 | Remapped | Perfect | NC_000002.12:g.(97 199309_?)_(?_97203 047)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,199,309 | 97,203,047 |
| essv25956143 | Remapped | Perfect | NC_000002.12:g.(97 199309_?)_(?_97203 047)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,199,309 | 97,203,047 |
| essv25959607 | Remapped | Perfect | NC_000002.12:g.(97 199309_?)_(?_97203 047)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,199,309 | 97,203,047 |
| essv25969750 | Remapped | Perfect | NC_000002.12:g.(97 199309_?)_(?_97203 047)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,199,309 | 97,203,047 |
| essv25974921 | Remapped | Perfect | NC_000002.12:g.(97 199309_?)_(?_97203 047)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,199,309 | 97,203,047 |
| essv25997832 | Remapped | Perfect | NC_000002.12:g.(97 199309_?)_(?_97203 047)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,199,309 | 97,203,047 |
| essv26020682 | Remapped | Perfect | NC_000002.12:g.(97 199309_?)_(?_97203 047)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,199,309 | 97,203,047 |
| essv26030872 | Remapped | Perfect | NC_000002.12:g.(97 199309_?)_(?_97203 047)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,199,309 | 97,203,047 |
| essv25939665 | Remapped | Perfect | NC_000002.12:g.(97 202193_?)_(?_97207 802)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,202,193 | 97,207,802 |
| essv25985752 | Remapped | Perfect | NC_000002.12:g.(97 202193_?)_(?_97207 802)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,202,193 | 97,207,802 |
| essv26022349 | Remapped | Perfect | NC_000002.12:g.(97 202193_?)_(?_97207 802)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,202,193 | 97,207,802 |
| essv25906158 | Remapped | Perfect | NC_000002.12:g.(97 204154_?)_(?_97207 896)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,204,154 | 97,207,896 |
| essv25904487 | Remapped | Perfect | NC_000002.12:g.(97 207914_?)_(?_97210 613)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,207,914 | 97,210,613 |
| essv25939883 | Remapped | Perfect | NC_000002.12:g.(97 207914_?)_(?_97210 613)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,207,914 | 97,210,613 |
| essv25948630 | Remapped | Perfect | NC_000002.12:g.(97 207914_?)_(?_97210 613)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,207,914 | 97,210,613 |
| essv25952617 | Remapped | Perfect | NC_000002.12:g.(97 207914_?)_(?_97210 613)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,207,914 | 97,210,613 |
| essv25964663 | Remapped | Perfect | NC_000002.12:g.(97 207914_?)_(?_97210 613)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,207,914 | 97,210,613 |
| essv25982136 | Remapped | Perfect | NC_000002.12:g.(97 207914_?)_(?_97210 613)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,207,914 | 97,210,613 |
| essv25990868 | Remapped | Perfect | NC_000002.12:g.(97 207914_?)_(?_97210 613)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,207,914 | 97,210,613 |
| essv25999613 | Remapped | Perfect | NC_000002.12:g.(97 207914_?)_(?_97210 613)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,207,914 | 97,210,613 |
| essv26001356 | Remapped | Perfect | NC_000002.12:g.(97 207914_?)_(?_97210 613)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,207,914 | 97,210,613 |
| essv26038064 | Remapped | Perfect | NC_000002.12:g.(97 207914_?)_(?_97210 613)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,207,914 | 97,210,613 |
| essv26004988 | Remapped | Perfect | NC_000002.12:g.(97 207914_?)_(?_97211 063)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,207,914 | 97,211,063 |
| essv25966494 | Submitted genomic | NC_000002.11:g.(97 846159_?)_(?_97849 879)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,846,159 | 97,849,879 | ||
| essv25899193 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv25902781 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv25920794 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv25937919 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv25954439 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv25970633 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv25973329 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv25982135 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv25990866 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv26001354 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv26004977 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv26017239 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv26018863 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv26030871 | Submitted genomic | NC_000002.11:g.(97 847364_?)_(?_97851 086)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,364 | 97,851,086 | ||
| essv26030473 | Submitted genomic | NC_000002.11:g.(97 847551_?)_(?_97903 800)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,847,551 | 97,903,800 | ||
| essv25897596 | Submitted genomic | NC_000002.11:g.(97 848401_?)_(?_97851 284)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,848,401 | 97,851,284 | ||
| essv25900929 | Submitted genomic | NC_000002.11:g.(97 848401_?)_(?_97851 284)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,848,401 | 97,851,284 | ||
| essv25939664 | Submitted genomic | NC_000002.11:g.(97 848401_?)_(?_97851 284)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,848,401 | 97,851,284 | ||
| essv25939872 | Submitted genomic | NC_000002.11:g.(97 848401_?)_(?_97851 284)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,848,401 | 97,851,284 | ||
| essv25944865 | Submitted genomic | NC_000002.11:g.(97 848401_?)_(?_97851 284)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,848,401 | 97,851,284 | ||
| essv25999612 | Submitted genomic | NC_000002.11:g.(97 848401_?)_(?_97851 284)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,848,401 | 97,851,284 | ||
| essv26034385 | Submitted genomic | NC_000002.11:g.(97 848401_?)_(?_97851 284)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,848,401 | 97,851,284 | ||
| essv25989022 | Submitted genomic | NC_000002.11:g.(97 849962_?)_(?_97853 713)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,849,962 | 97,853,713 | ||
| essv25895752 | Submitted genomic | NC_000002.11:g.(97 853401_?)_(?_97856 100)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,853,401 | 97,856,100 | ||
| essv25957832 | Submitted genomic | NC_000002.11:g.(97 853401_?)_(?_97856 100)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,853,401 | 97,856,100 | ||
| essv25971630 | Submitted genomic | NC_000002.11:g.(97 853401_?)_(?_97856 100)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,853,401 | 97,856,100 | ||
| essv25986166 | Submitted genomic | NC_000002.11:g.(97 853851_?)_(?_97856 100)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,853,851 | 97,856,100 | ||
| essv26030600 | Submitted genomic | NC_000002.11:g.(97 853851_?)_(?_97856 100)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,853,851 | 97,856,100 | ||
| essv25966495 | Submitted genomic | NC_000002.11:g.(97 853851_?)_(?_97856 550)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,853,851 | 97,856,550 | ||
| essv25937920 | Submitted genomic | NC_000002.11:g.(97 854301_?)_(?_97856 550)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,854,301 | 97,856,550 | ||
| essv25964333 | Submitted genomic | NC_000002.11:g.(97 854301_?)_(?_97856 550)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,854,301 | 97,856,550 | ||
| essv25973330 | Submitted genomic | NC_000002.11:g.(97 858653_?)_(?_97881 267)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,858,653 | 97,881,267 | ||
| essv25937921 | Submitted genomic | NC_000002.11:g.(97 865046_?)_(?_97868 784)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,865,046 | 97,868,784 | ||
| essv25954689 | Submitted genomic | NC_000002.11:g.(97 865046_?)_(?_97868 784)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,865,046 | 97,868,784 | ||
| essv25956143 | Submitted genomic | NC_000002.11:g.(97 865046_?)_(?_97868 784)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,865,046 | 97,868,784 | ||
| essv25959607 | Submitted genomic | NC_000002.11:g.(97 865046_?)_(?_97868 784)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,865,046 | 97,868,784 | ||
| essv25969750 | Submitted genomic | NC_000002.11:g.(97 865046_?)_(?_97868 784)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,865,046 | 97,868,784 | ||
| essv25974921 | Submitted genomic | NC_000002.11:g.(97 865046_?)_(?_97868 784)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,865,046 | 97,868,784 | ||
| essv25997832 | Submitted genomic | NC_000002.11:g.(97 865046_?)_(?_97868 784)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,865,046 | 97,868,784 | ||
| essv26020682 | Submitted genomic | NC_000002.11:g.(97 865046_?)_(?_97868 784)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,865,046 | 97,868,784 | ||
| essv26030872 | Submitted genomic | NC_000002.11:g.(97 865046_?)_(?_97868 784)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,865,046 | 97,868,784 | ||
| essv25939665 | Submitted genomic | NC_000002.11:g.(97 867930_?)_(?_97873 539)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 97,867,930 | 97,873,539 |