fix: update T2T consortia text (#4059) (#4060)

explorer/files/anvil-catalog/files/consortia/t2t.mdx

@@ -5,5 +5,3 @@ Leveraging PacBio HiFi sequencing and Oxford Nanopore ultra-long reads, the CHM1
 CHM13v1 unlocks complex regions of the genome for clinical and functional study. Additionally, the T2T-CHRY Workspace utilizes the T2T-CHM13v2.0, which provides the first complete sequence for a human Y chromosome from a separate donor (HG002).
 
 T2T-CHM13v2.0 was also used as a reference genome for investigating short-read variant calling, incorporating data from the 1000 Genomes Project and the Simons Genome Diversity Project. Another effort from the T2T consortium is the T2T-GreatApes Project which employs PacBio HiFi and Oxford Nanopore ultra-long reads, advancing our understanding of great ape genomics. It evaluates the impact of T2T-chrXY assemblies on read alignments and variant calling across 129 individuals from 11 great ape subspecies, providing reference genomes for various ape species.
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-The 1000 Genomes Project, launched in January 2008, is an international research effort to establish variation profiles across the human population. This open access data set continues to be a valuable resource to geneticists.