PMC:4067558 / 10160-10636 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/4067558","sourcedb":"PMC","sourceid":"4067558","source_url":"https://www.ncbi.nlm.nih.gov/pmc/4067558","text":"Secondary analyses included comparisons of CNV number, length, and intersected gene number between our 102 de novo CNVs identified in affected subjects and the 76 de novo CNVs in control subjects of two published data sets: (1) 17 de novo CNVs identified in 15 unaffected siblings from 872 families with a single ASD-affected offspring and an unaffected sibling from the Simons Simplex Collection4 and (2) 59 de novo CNVs detected in 57 out of 2,623 Icelandic control trios.31","tracks":[{"project":"2_test","denotations":[{"id":"24768552-21658581-2047100","span":{"begin":396,"end":397},"obj":"21658581"},{"id":"24768552-22083728-2047101","span":{"begin":474,"end":476},"obj":"22083728"}],"attributes":[{"subj":"24768552-21658581-2047100","pred":"source","obj":"2_test"},{"subj":"24768552-22083728-2047101","pred":"source","obj":"2_test"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"2_test","color":"#ecc393","default":true}]}]}}