17q12 Knowledge Basedeletion syndrome · static snapshot
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New publication Genes & inheritance 1 supporting source confidence 97% novelty 75%

Copy number variant association analysis in 94,730 Chinese adults reveals loci influencing anthropometric and cardiometabolic traits

Copy-number variants (CNVs) represent an important source of genetic variation that can influence complex traits and disease risk by altering gene dosage, disrupting coding sequence, or modifying regulatory elements.

How this was derived

Indexed from **openalex** on 2026-11-13 (relevance 1.00, tier peer_reviewed).

Generated 2026-11-13, last changed yesterday. Dedup key newdoc:517. 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)

Novel associations include random plasma glucose at 8p23.1 (β = -0.29 SD, P = 5.40×10⁻) and 14q11.2 (β = +0.43 SD, P = 8.41×10⁻), diastolic blood pressure at 7p21.1 (β = +0.75 SD, P = 5.25×10⁻), and duplication-associated reductions in body fat percentage at 12p12.1 (β = -0.74 SD, P = 8.11×10⁻) and 17q12 (β = -0.56 SD, P = 7.36×10⁻).

Supporting documents (1)

DocumentSourcePublishedSeenRelevance
Copy number variant association analysis in 94,730 Chinese adults r... openalex 2026-08-13 yesterday 1.00