Publication Details

Results for Long2019:

Title The Clinical and Genetic Features of Co-occurring Epilepsy and Autism Spectrum Disorder in Chinese Children
AuthorsLong, S., Zhou, H., Li, S., Wang, T., Ma, Y., Li, C., Zhou, Y., Zhou, S., Wu, B., Wang, Y.
TechnologyTargeted sequencing, Whole exome sequencing
Variant sourceTable S1: gene and CNV
CohortsChinese children
Subject count32
The number of subjects for this study could not be determined directly from the variant data; the value given is that reported by the authors in the publication.
Variant event count33
Curation notesView
Breakdown by exonic function
FunctionVariant Count
frameshift deletion2
nonframeshift deletion1
nonframeshift substitution1
nonsynonymous SNV22

What am I looking at?

Summary: Information from the literature piece (e.g. Author, Publisher, DOI) and the study experimental design (e.g. sample size, source of probands, sequencing technology.) For a full list of sources of variants, be sure to check out the publications page. Documentation and description of our work can be found on the help page.

Breakdown by exonic function: We annotated the variants with an effect prediction using ANNOVAR. The functions are categories of variants, such as frameshift variants (i.e. frameshift_elongation (SO:0001909)), loss/gain of stop codon, SNVs and non-frameshift variants. See the full list of possible annotations for exonic variants in the documentation.