17q12, explained for kidsdeletion syndrome · static snapshot
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A number from a study Learning, talking and behaviour 1 supporting source confidence 97% novelty 60%

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 indiv

A source reports “075 individuals” in the context of neurodevelopment: “Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.”

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Generated 2026-11-14, last changed today. Dedup key freq:075 individuals. The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.

Evidence (1 quote)

17q12 Recurrent Deletion Syndrome in Childhood peer_reviewed · published 2025-01-01 · live page
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.

Supporting documents (1)

StorySourcePublishedSeenRelevance
17q12 Recurrent Deletion Syndrome in Childhood pmc 2025-01-01 yesterday 1.00