17q12, explained for kidsdeletion syndrome · static snapshot
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An additional genetic analysis was reported for 15 individuals with recurrent duplications and duplications larger than

A source reports “15 individuals” in the context of general: “An additional genetic analysis was reported for 15 individuals with recurrent duplications and duplications larger than 1 Mb: three had single nucleotide variants of uncertain clinical significance, one had a pathogenic 15q11.2 deletion, and the remaining 11 h”

How this was derived

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Generated 2026-11-13, last changed yesterday. Dedup key freq:15 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)

An additional genetic analysis was reported for 15 individuals with recurrent duplications and duplications larger than 1 Mb: three had single nucleotide variants of uncertain clinical significance, one had a pathogenic 15q11.2 deletion, and the remaining 11 had a negative ID next generation sequencing (ID NGS) panel or exome sequencing (ES).

Supporting documents (1)

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Delineation of the Genetic Architecture and Clinical Polymorphism o... pmc 2024-01-01 yesterday 1.00